Single-center, randomized, double-blind, placebo-controlled, single ascending dose, safety and tolerability study of TNX-201 capsules in healthy volunteers.
Single-center, randomized, double-blind, placebo-controlled, single ascending dose, safety and tolerability study of TNX-201 capsules in healthy volunteers. Three successive cohorts are planned with doses of TNX-201 capsules, 35 mg, 70 mg, and 140 mg, respectively. Each cohort will consist of 15 subjects, and subjects will be randomly assigned to TNX-201, racemic isometheptene, or placebo capsules.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
27
Drug: TNX-201 35 mg
Drug: TNX-201 70 mg
Drug: TNX-201 140 mg
Plasma levels of isometheptene or metabolites.
Time frame: 60 minutes pre-dose and multiple timepoints up to 48 hours post-dose
Number of Adverse events
Time frame: 60 minutes pre-dose and multiple timepoints up to 48 hours post-dose
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Active Comparator: Racemic isometheptene 70 mg
Drug: Placebo